MeSH2022Disease Find_IDs Find_Terms Annotation
manager
language -
license -
created at 2021-12-15 00:03:01 UTC
updated at 2021-12-16 08:13:02 UTC
MeSH® Disease Terms

Source: ASCII MeSH files (d2022.bin and c2022.bin) downloaded from https://nlmpubs.nlm.nih.gov/projects/mesh/MESH_FILES/asciimesh/at Dec 14 16:16 (JST)

Method:
step1: Selected records that have tree numbers (MN) beginning with 'C' and took preferred term (MH) and synonyms (ENTRY and PRINT ENTRY: terms at the left of the first vertical bars), and the corresponding MeSH Unique IDs (UI) from the descriptor file (d2022.bin).

step2: Selected records that have corresponding descriptor (HM) that corresponds to an entry in step1, and took preferred term (NM) and synonyms (SY), and the corresponding MeSH Unique IDs (UI) from the supplementary records file (c2022.bin).
80,878 entries
Label
Id
CGD, autosomal recessive cytochrome b-positive, type II C565531
autosomal recessive cytochrome b-positive, type II CGD C565531
chronic, autosomal recessive, cytochrome b-positive, type II granulomatous disease C565531
chronic, due to NCF2 deficiency granulomatous disease C565531
deficiency of neutrophil cytosol factor 2 C565531
deficiency of p67-phox C565531
granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II C565531
granulomatous disease, chronic, due to NCF2 deficiency C565531
neutrophil cytosol factor 2, deficiency of C565531
p67-phox, deficiency of C565531